Nature of Interactions of Amino Acids with Bare Magnetite Nanoparticles

被引:146
作者
Schwaminger, Sebastian P. [1 ]
Garcia, Paula Fraga [1 ]
Merck, Georg K. [1 ]
Bodensteiner, Fabian A. [1 ]
Heissler, Stefan [2 ]
Guenther, Sebastian [3 ]
Berensmeier, Sonja [1 ]
机构
[1] Tech Univ Munich, Bioseparat Engn Grp, D-85748 Garching, Germany
[2] Karlsruhe Inst Technol, Inst Funct Interfaces, D-76344 Eggenstein Leopoldshafen, Germany
[3] Tech Univ Munich, Dept Chem, D-85748 Garching, Germany
关键词
IRON-OXIDE NANOPARTICLES; TIO2; NANOPARTICLES; PROTEIN RECOVERY; FORMIC-ACID; L-LYSINE; ADSORPTION; SURFACE; CYSTEINE; PH; SEPARATION;
D O I
10.1021/acs.jpcc.5b07195
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Owing to their chemical and magnetic properties, magnetite nanoparticles are an interesting adsorbing material for biomolecules. The understanding of the interactions of simple biomolecules with inorganic nanoparticles is an important approach for research on the bio-nano interface and can constitute the fundamentals to manifold applications in biotechnology, medicine and catalysis. The aim of the work presented here is to compare the interaction of seven different amino acids (L-alanine, L-cysteine, L-glutamic acid, glycine, L-histidine, L-lysine, and L-serine) with magnetite nanoparticles in a colloidal system at pH 6. We investigate the influence of the side chain on the adsorption at a magnetite-water interface with incubation experiments. Attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and simultaneous thermal analysis (STA) reveal deeper insights into the interactions of amino acids with magnetite nanopartides. The amino acids that contain polar side chains adsorb on the nanopartides to a high degree. Cysteine demonstrates the highest adsorption capacity and the formation of cystine is observed. ATR-FTIR spectroscopy results indicate a strong influence of the carboxyl group and side chains on the binding mechanism of amino acids at the iron oxide surface. Our investigation offers novel knowledge into adsorption behavior at the bio-nano interface.
引用
收藏
页码:23032 / 23041
页数:10
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